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FDA 510(k)

INTELIJET SUCTION SUPPLY

K-Number: K922176 · 1992-11-18

ApplicantSmith & Nephew Dyonics, Inc.
Decision Date1992-11-18
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INTELIJET SUCTION SUPPLY is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Dyonics, Inc.. It received FDA 510(k) clearance on 1992-11-18 under 510(k) number K922176. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTELIJET SUCTION SUPPLY?

INTELIJET SUCTION SUPPLY is a medical device that received FDA 510(k) clearance on 1992-11-18. The listed applicant is Smith & Nephew Dyonics, Inc.. The 510(k) number is K922176.

When did INTELIJET SUCTION SUPPLY receive FDA 510(k) clearance?

INTELIJET SUCTION SUPPLY received FDA 510(k) clearance on 1992-11-18, under 510(k) number K922176.

Who is the listed applicant for INTELIJET SUCTION SUPPLY?

The FDA 510(k) record lists Smith & Nephew Dyonics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTELIJET SUCTION SUPPLY?

The FDA product code for INTELIJET SUCTION SUPPLY is BTA.

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Related Devices (Code: BTA)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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